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402600008: xerodermie bij genetisch syndroom (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1770524011 Xeroderma in genetic syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1781717014 Xeroderma in genetic syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
11705051000146111 xerodermie bij genetisch syndroom (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
11705061000146114 xeroderma bij genetisch syndroom nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
11705071000146115 xerodermie bij genetisch syndroom nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Xeroderma in genetic syndrome (disorder) Is a Xeroderma true Inferred relationship Some
Xeroderma in genetic syndrome (disorder) Finding site Skin structure false Inferred relationship Some 1
Xeroderma in genetic syndrome (disorder) Associated morphology Papulovesicular rash false Inferred relationship Some 1
Xeroderma in genetic syndrome (disorder) Has definitional manifestation Abnormal keratinization false Inferred relationship Some
Xeroderma in genetic syndrome (disorder) Finding site Structure of skin region false Inferred relationship Some
Xeroderma in genetic syndrome (disorder) Finding site Skin structure true Inferred relationship Some 3
Xeroderma in genetic syndrome (disorder) Has interpretation Abnormal false Inferred relationship Some 1
Xeroderma in genetic syndrome (disorder) Interprets Keratinization false Inferred relationship Some 1
Xeroderma in genetic syndrome (disorder) Interprets Moistness of skin false Inferred relationship Some 2
Xeroderma in genetic syndrome (disorder) Interprets Moistness of skin true Inferred relationship Some 1
Xeroderma in genetic syndrome (disorder) Has interpretation Decreased true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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